FDA Inspection 1193488 — Medifactia AB

Medifactia AB — FEI 3015871081

The FDA completed an inspection of Medifactia AB on Nov 14, 2022 in Stockholm. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Nov 14, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Stockholm (Sweden)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.